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Clinicopathologic Analysis of Coxsackievirus A6 New Variant Induced Widespread Mucocutaneous Bullous Reactions Mimicking Severe Cutaneous Adverse Reactions

The Journal of infectious diseases, 2013-12, Vol.208 (12), p.1968-1978

2013

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HLA-B5801 Allele as a Genetic Marker for Severe Cutaneous Adverse Reactions Caused by Allopurinol

Proceedings of the National Academy of Sciences - PNAS, 2005-03, Vol.102 (11), p.4134-4139

2005

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Direct interaction between HLA-B and carbamazepine activates T cells in patients with Stevens-Johnson syndrome

Journal of allergy and clinical immunology, 2012-06, Vol.129 (6), p.1562-1569.e5

2012

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ENU mutagenesis identifies mice with cardiac fibrosis and hepatic steatosis caused by a mutation in the mitochondrial trifunctional protein β-subunit

Human molecular genetics, 2006-12, Vol.15 (24), p.3569-3577

2006

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The Function of HLA-B13:01 Involved in the Pathomechanism of Dapsone-Induced Severe Cutaneous Adverse Reactions

Journal of investigative dermatology, 2018-07, Vol.138 (7), p.1546-1554

2018

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Shared and restricted T-cell receptor use is crucial for carbamazepine-induced Stevens-Johnson syndrome

Journal of allergy and clinical immunology, 2011-12, Vol.128 (6), p.1266-1276.e11

2011

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Genetic variants associated with phenytoin-related severe cutaneous adverse reactions

JAMA : the journal of the American Medical Association, 2014-08, Vol.312 (5), p.525

2014

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Genetic susceptibility to carbamazepine-induced cutaneous adverse drug reactions

Pharmacogenetics and genomics, 2006-04, Vol.16 (4), p.297-306

2006

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A new nucleic acid–based agent inhibits cytotoxic T lymphocyte–mediated immune disorders

Journal of allergy and clinical immunology, 2013-09, Vol.132 (3), p.713-722.e11

2013

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Human leukocyte antigens and drug hypersensitivity

Current opinion in allergy and clinical immunology, 2007-08, Vol.7 (4), p.317-323

2007

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HLA-B1502-bound peptides : Implications for the pathogenesis of carbamazepine-induced Stevens-Johnson syndrome

Journal of allergy and clinical immunology, 2007-10, Vol.120 (4), p.870-877

2007

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Severe Cutaneous Adverse Reactions Related to Systemic Antibiotics

Clinical infectious diseases, 2014-05, Vol.58 (10), p.1377-1385

2014

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A Single Nucleotide Polymorphism Fine Mapping Study of Chromosome 1q42.1 Reveals the Vulnerability Genes for Schizophrenia, GNPAT and DISC1: Association with Impairment of Sustained Attention

Biological psychiatry (1969), 2006-09, Vol.60 (6), p.554-562

2006

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Longitudinal evaluation of an N-ethyl-N-nitrosourea-created murine model with normal pressure hydrocephalus

PloS one, 2009-11, Vol.4 (11), p.e7868-e7868

2009

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Genetic variation in renin predicts the effects of thiazide diuretics

European journal of clinical investigation, 2011-08, Vol.41 (8), p.828-835

2011

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HTF9C gene of 22q11.21 region associates with schizophrenia having deficit-sustained attention

Psychiatric genetics, 2007-12, Vol.17 (6), p.333-338

2007

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RASD2, MYH9, and CACNG2 Genes at Chromosome 22q12 Associated with the Subgroup of Schizophrenia with Non-Deficit in Sustained Attention and Executive Function: Neurodevelopment and the Transition from Schizophrenia Prodrome to Schizophrenia

Biological psychiatry (1969), 2008, Vol.64 (9), p.789-796

2008

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Clients driving innovation

2009

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A single nucleotide polymorphism fine mapping study of chromosome 1q42.1 reveals the vulnerability genes for schizophrenia, GNPAT and DISC1 : Association with impairment of sustained attention: Molecular mechanisms of schizophrenia

Biological psychiatry (1969), 2006, Vol.60 (6), p.554-562

2006

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Study on the Localization of Instrumentation Installation Materials for AP1000

Proceedings of The 20th Pacific Basin Nuclear Conference, 2017, p.283-290

2017

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Clinicopathologic features of skin reactions to temporary tattoos and analysis of possible causes

Archives of dermatology (1960), 2002-01, Vol.138 (1), p.88

2002

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Datenrechtsgesetz 3.0: Der gesetzgeberische Ausblick des Datenrechts

Lian, Yuming

2022

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The Paradoxical Role of Uric Acid in Osteoporosis

Nutrients, 2019-09, Vol.11 (9), p.2111

2019

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Carbamazepine-Induced Toxic Effects and HLA-B1502 Screening in Taiwan

The New England journal of medicine, 2011-03, Vol.364 (12), p.1126-1133

2011

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A late embryogenesis abundant protein HVA1 regulated by an inducible promoter enhances root growth and abiotic stress tolerance in rice without yield penalty

Plant biotechnology journal, 2015-01, Vol.13 (1), p.105-116

2015

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Clinicopathologic Analysis of Coxsackievirus A6 New Variant Induced Widespread Mucocutaneous Bullous Reactions Mimicking Severe Cutaneous Adverse Reactions

HLA-B5801 Allele as a Genetic Marker for Severe Cutaneous Adverse Reactions Caused by Allopurinol

Direct interaction between HLA-B and carbamazepine activates T cells in patients with Stevens-Johnson syndrome

ENU mutagenesis identifies mice with cardiac fibrosis and hepatic steatosis caused by a mutation in the mitochondrial trifunctional protein β-subunit

The Function of HLA-B13:01 Involved in the Pathomechanism of Dapsone-Induced Severe Cutaneous Adverse Reactions

Shared and restricted T-cell receptor use is crucial for carbamazepine-induced Stevens-Johnson syndrome

Genetic variants associated with phenytoin-related severe cutaneous adverse reactions

Genetic susceptibility to carbamazepine-induced cutaneous adverse drug reactions

A new nucleic acid–based agent inhibits cytotoxic T lymphocyte–mediated immune disorders

Human leukocyte antigens and drug hypersensitivity

HLA-B1502-bound peptides : Implications for the pathogenesis of carbamazepine-induced Stevens-Johnson syndrome

Severe Cutaneous Adverse Reactions Related to Systemic Antibiotics

A Single Nucleotide Polymorphism Fine Mapping Study of Chromosome 1q42.1 Reveals the Vulnerability Genes for Schizophrenia, GNPAT and DISC1: Association with Impairment of Sustained Attention

Longitudinal evaluation of an N-ethyl-N-nitrosourea-created murine model with normal pressure hydrocephalus

Genetic variation in renin predicts the effects of thiazide diuretics

HTF9C gene of 22q11.21 region associates with schizophrenia having deficit-sustained attention

RASD2, MYH9, and CACNG2 Genes at Chromosome 22q12 Associated with the Subgroup of Schizophrenia with Non-Deficit in Sustained Attention and Executive Function: Neurodevelopment and the Transition from Schizophrenia Prodrome to Schizophrenia

Clients driving innovation

A single nucleotide polymorphism fine mapping study of chromosome 1q42.1 reveals the vulnerability genes for schizophrenia, GNPAT and DISC1 : Association with impairment of sustained attention: Molecular mechanisms of schizophrenia

Study on the Localization of Instrumentation Installation Materials for AP1000

Clinicopathologic features of skin reactions to temporary tattoos and analysis of possible causes

Datenrechtsgesetz 3.0: Der gesetzgeberische Ausblick des Datenrechts

The Paradoxical Role of Uric Acid in Osteoporosis

Carbamazepine-Induced Toxic Effects and HLA-B1502 Screening in Taiwan

A late embryogenesis abundant protein HVA1 regulated by an inducible promoter enhances root growth and abiotic stress tolerance in rice without yield penalty

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